A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421594



Internal ID200660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1278885..1301003hg38UCSC Ensembl
chrX:1397778..1419896hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3822119
hg1922119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738773
Samples
Known GenesCSF2RA, MIR3690, MIR3690-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421594
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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